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HARVARD Citation
Olinger, E. et al. (2022). Biallelic variants in TTC21B as a rare cause of early‐onset arterial hypertension and tubuloglomerular kidney disease. American journal of medical genetics. 190 (1), pp. 109-120. [Online].
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Olinger, E. et al. (2022). Biallelic variants in TTC21B as a rare cause of early‐onset arterial hypertension and tubuloglomerular kidney disease. American journal of medical genetics. 190 (1), pp. 109-120. [Online].